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The Prognostic Value of Soluble ST2 in Adults with Pulmonary Hypertension
Soluble ST2 (sST2) is upregulated in response to myocardial stress and may serve as biomarker in adults with pulmonary hypertension (PH). This prospective cohort study investigated sST2 levels and its association with echocardiographic and hemodynamic measures, and adverse clinical outcomes in adult...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832164/ https://www.ncbi.nlm.nih.gov/pubmed/31547136 http://dx.doi.org/10.3390/jcm8101517 |
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author | Geenen, Laurie W. Baggen, Vivan J. M. Kauling, Robert M. Koudstaal, Thomas Boomars, Karin A. Boersma, Eric Roos-Hesselink, Jolien W. van den Bosch, Annemien E. |
author_facet | Geenen, Laurie W. Baggen, Vivan J. M. Kauling, Robert M. Koudstaal, Thomas Boomars, Karin A. Boersma, Eric Roos-Hesselink, Jolien W. van den Bosch, Annemien E. |
author_sort | Geenen, Laurie W. |
collection | PubMed |
description | Soluble ST2 (sST2) is upregulated in response to myocardial stress and may serve as biomarker in adults with pulmonary hypertension (PH). This prospective cohort study investigated sST2 levels and its association with echocardiographic and hemodynamic measures, and adverse clinical outcomes in adults with PH of different etiologies. sST2 was measured during the diagnostic right heart catheterization for PH, in adult patients enrolled between May 2012 and October 2016. PH due to left heart failure was excluded. The association between sST2 and a primary endpoint composed of death or lung transplantation and a secondary composite endpoint including death, lung transplantation or heart failure, was investigated using Cox regression with adjustment for NT-proBNP. In total 104 patients were included (median age was 59 years, 66% woman, 51% pulmonary arterial hypertension). Median sST2 was 28 [IQR 20–46] ng/mL. Higher sST2 was associated with worse right ventricular dysfunction and higher mean pulmonary and right atrial pressures. Median follow-up was 3.3 [IQR 2.3–4.6] years. The primary and secondary endpoint occurred in 33 (31.7%) and 43 (41.3%) patients, respectively. sST2 was significantly associated with both endpoints (HR per 2-fold higher value 1.53, 95%CI 1.12–2.07, p = 0.007 and 1.45, 95%CI 1.10–1.90, p = 0.008, respectively). However, after adjustment for NT-proBNP, both associations did not reach statistical significance. In conclusions, higher sST2 levels are associated with more severe PH and right ventricular dysfunction and yields prognostic value in adults with PH, although not independently of NT-proBNP. |
format | Online Article Text |
id | pubmed-6832164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68321642019-11-20 The Prognostic Value of Soluble ST2 in Adults with Pulmonary Hypertension Geenen, Laurie W. Baggen, Vivan J. M. Kauling, Robert M. Koudstaal, Thomas Boomars, Karin A. Boersma, Eric Roos-Hesselink, Jolien W. van den Bosch, Annemien E. J Clin Med Article Soluble ST2 (sST2) is upregulated in response to myocardial stress and may serve as biomarker in adults with pulmonary hypertension (PH). This prospective cohort study investigated sST2 levels and its association with echocardiographic and hemodynamic measures, and adverse clinical outcomes in adults with PH of different etiologies. sST2 was measured during the diagnostic right heart catheterization for PH, in adult patients enrolled between May 2012 and October 2016. PH due to left heart failure was excluded. The association between sST2 and a primary endpoint composed of death or lung transplantation and a secondary composite endpoint including death, lung transplantation or heart failure, was investigated using Cox regression with adjustment for NT-proBNP. In total 104 patients were included (median age was 59 years, 66% woman, 51% pulmonary arterial hypertension). Median sST2 was 28 [IQR 20–46] ng/mL. Higher sST2 was associated with worse right ventricular dysfunction and higher mean pulmonary and right atrial pressures. Median follow-up was 3.3 [IQR 2.3–4.6] years. The primary and secondary endpoint occurred in 33 (31.7%) and 43 (41.3%) patients, respectively. sST2 was significantly associated with both endpoints (HR per 2-fold higher value 1.53, 95%CI 1.12–2.07, p = 0.007 and 1.45, 95%CI 1.10–1.90, p = 0.008, respectively). However, after adjustment for NT-proBNP, both associations did not reach statistical significance. In conclusions, higher sST2 levels are associated with more severe PH and right ventricular dysfunction and yields prognostic value in adults with PH, although not independently of NT-proBNP. MDPI 2019-09-20 /pmc/articles/PMC6832164/ /pubmed/31547136 http://dx.doi.org/10.3390/jcm8101517 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Geenen, Laurie W. Baggen, Vivan J. M. Kauling, Robert M. Koudstaal, Thomas Boomars, Karin A. Boersma, Eric Roos-Hesselink, Jolien W. van den Bosch, Annemien E. The Prognostic Value of Soluble ST2 in Adults with Pulmonary Hypertension |
title | The Prognostic Value of Soluble ST2 in Adults with Pulmonary Hypertension |
title_full | The Prognostic Value of Soluble ST2 in Adults with Pulmonary Hypertension |
title_fullStr | The Prognostic Value of Soluble ST2 in Adults with Pulmonary Hypertension |
title_full_unstemmed | The Prognostic Value of Soluble ST2 in Adults with Pulmonary Hypertension |
title_short | The Prognostic Value of Soluble ST2 in Adults with Pulmonary Hypertension |
title_sort | prognostic value of soluble st2 in adults with pulmonary hypertension |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832164/ https://www.ncbi.nlm.nih.gov/pubmed/31547136 http://dx.doi.org/10.3390/jcm8101517 |
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